A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375569



Internal ID21033122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:178398376..178439243hg38UCSC Ensembl
chr3:178116164..178157031hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3840868
hg1940868
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211507
Samples
Known GenesLINC01014
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375569
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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